This Regulatory Affairs Specialist II will work on-site out of our Atlanta, GA location in our Heart Failure Division. As an individual contributor, this position performs specialized level work assignments and/or analyses, evaluation, preparation, and submission of documentation for the worldwide r...
As an individual contributor, the Principal Regulatory Affairs Specialist is responsible for providing regulatory guidance to cross-functional partners, developing global regulatory strategies for new and modified Class III devices and preparing and submitting regulatory submissions in the US, EU an...
As an individual contributor, the Principal Regulatory Affairs Specialist is responsible for providing regulatory guidance to cross-functional partners, developing global regulatory strategies for new and modified Class III devices and preparing and submitting regulatory submissions in the US, EU an...
As an individual contributor, the Senior Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient and compliant business processes and environment. Senior Regulatory Affairs Specialist. Acts as a regulatory representative on core product development teams...
We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. ...
As an individual contributor, this position performs specialized level work assignments and/or analyses, evaluation, preparation, and submission of documentation for the worldwide regulatory registration, ensuring products and procedures comply with regulatory agency specifications. Prepares robust ...
Kemira Product Safety and Regulatory Affairs (PSRA) drives the global execution of product safety and product regulatory compliance related activities, and proactively contributes to Kemira product stewardship through lifecycle approach. We are seeking a skilled professional to join the company...
As an individual contributor, the Principal Regulatory Affairs Specialist is responsible for providing regulatory guidance to cross-functional partners, developing global regulatory strategies for new and modified Class III devices and preparing and submitting regulatory submissions in the US, EU an...
Assists regulatory team (Regulatory Specialist II and III) in research efforts by facilitating the protocol approval process and maintaining documentation of regulatory compliance throughout the trial's duration for research studies involving human subjects. The Clinical Trials Regulatory Specialist...
Environmental Regulatory Specialist. For the Managing Consultant, Environmental Regulatory Specialist (Senior Level) position, we anticipate the annual base pay of $76,000 – $94,860 (USD). Federal Energy Regulatory Commission (FERC). Research, analyze and compile data for permit applications and rep...
The Regulatory Affairs Specialist will reside within strategic business unit, Huber Specialty Minerals (HSM), at Huber Engineered Materials (HEM). Develops and supervises global Regulatory Affairs support function to leverage Subject Matter Expertise (SME) for completion of Customer requests, Regula...
Varian is seeking an Internal Auditor Program Manager. As the Internal Auditor Program Manager will work cross-functionally with global teams to maintain certifications and a robust quality system, while fostering continuous improvement through training and best practice sharing. Responsible for exe...
Manager, Regulatory Affairs Labeling – Permanent – Georgia, North Carolina or Massachusetts. Proclinical is seeking a remote Manager, Regulatory Affairs Labeling for a global biopharmaceutical company with locations in Georgia, North Carolina and Massachusetts. The Manager, Regulatory Affairs Labeli...
As a Quality Assurance Specialist II, you will provide Quality support and oversight to Filling Operations; Identify and assess regulatory and quality risks in activities and processes according to regulatory agency rules, guidelines and quality practices. This is a role that reports to the Quality ...
Rohadfox is seeking a dedicated Quality Assurance Specialist to oversee and coordinate quality control efforts for our joint venture on large multimillion-dollar transportation projects. As a Quality Assurance Specialist at our organization, you will contribute to ensuring that our projects not only...
Work with client project manager to ensure understanding of all project activities, schedules and deliverables, act as resource for questions, and manage expectations. PROJECT MANAGER (PMP CERTIFIED). At least one scenario of a new system being built in which you project managed it from project kick...
Owing to exceptional growth and increased investment, our client is are seeking an accomplished Construction Project Manager to oversee multiple large-scale data center projects. As a Data Center Construction Project Manager, you will lead the end-to-end execution of data center construction project...
Ensures compliance of MARTA’s Drug & Alcohol Program (Drug and Alcohol Policy and Department of Transportation (DOT)/FTA regulations 49 Parts 40 and 655) in collaboration with the business unit's OMS Specialist. Conducts safety-sensitive contractor Drug & Alcohol oversight, including review and iden...
Discover Your Career at Emory University:.Emory University is a leading research university that fosters excellence and attracts world-class talent to innovate today and prepare leaders for the future.We welcome candidates who can contribute to the diversity and excellence of our academic community....
Internal and Vendor Quality Assurance Specialist. Kinetic's internal quality processes for service delivery, the technician assistance centers and manage our external vendor quality programs. The ideal candidate will be responsible for ensuring compliance with company quality standards as well as as...
The Program Manager defines the objectives and develops suitable strategies for the program. Develops a program evaluation framework to assess the strengths of the program and to identify areas for improvement. The career progression begins with assignments to formulate, organize, and monitor inter-...
Come join a company that strives for Extraordinary People and Exceptional Performance! Chenega Enterprise Systems & Solutions, LLC, a Chenega Professional Services’ company, is looking for a CLIA Compliance Data Analyst to support the Laboratory Quality Office (LQO) which provides strategic guidance...
Senior/Lead Technical Project Manager. Solugenix is assisting a client in their search for a Senior/Lead Technical Project Manager for a critical initiative Payments product. Matrix delivery/project team management. ...
Taxpayer Services Return Integrity and Compliance Services-Refundable Credits Examination Operations (RCEO). This experience may have been gained through work experience as a project/program manager, team lead or project/program lead, technical advisor, or senior specialist/analyst that included man...
The Product Safety & Regulatory Compliance Team is seeking a Regulatory Affairs Manager to join our team. Experience working in regulatory compliance, chemical control, regulatory affairs, environmental, laboratory or product safety in the agriculture industry. Bring regulatory knowledge and exp...